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具有增强的一氧化碳氧化催化性能的CeO-MO(M = Cu、Co、Ni)复合蛋黄壳纳米球的制备。

Fabrication of CeO-MO (M = Cu, Co, Ni) composite yolk-shell nanospheres with enhanced catalytic properties for CO oxidation.

作者信息

Liu Ling, Shi Jingjing, Cao Hongxia, Wang Ruiyu, Liu Ziwu

机构信息

Low Carbon Energy Institute, China University of Mining and Technology, Xuzhou 221008, People's Republic of China.

Key Laboratory of Coal-Based CO2 Capture and Geological Storage of Jiangsu Province, China University of Mining and Technology, Xuzhou 221008, People's Republic of China.

出版信息

Beilstein J Nanotechnol. 2017 Nov 16;8:2425-2437. doi: 10.3762/bjnano.8.241. eCollection 2017.

Abstract

CeO-MO (M = Cu, Co, Ni) composite yolk-shell nanospheres with uniform size were fabricated by a general wet-chemical approach. It involved a non-equilibrium heat-treatment of Ce coordination polymer colloidal spheres (Ce-CPCSs) with a proper heating rate to produce CeO yolk-shell nanospheres, followed by a solvothermal treatment of as-synthesized CeO with M(CHCOO) in ethanol solution. During the solvothermal process, highly dispersed MO species were decorated on the surface of CeO yolk-shell nanospheres to form CeO-MO composites. As a CO oxidation catalyst, the CeO-MO composite yolk-shell nanospheres showed strikingly higher catalytic activity than naked CeO due to the strong synergistic interaction at the interface sites between MO and CeO. Cycling tests demonstrate the good cycle stability of these yolk-shell nanospheres. The initial concentration of M(CHCOO)·HO in the synthesis process played a significant role in catalytic performance for CO oxidation. Impressively, complete CO conversion as reached at a relatively low temperature of 145 °C over the CeO-CuO -2 sample. Furthermore, the CeO-CuO catalyst is more active than the CeO-CoO and CeO-NiO catalysts, indicating that the catalytic activity is correlates with the metal oxide. Additionally, this versatile synthesis approach can be expected to create other ceria-based composite oxide systems with various structures for a broad range of technical applications.

摘要

通过一种通用的湿化学方法制备了尺寸均匀的CeO-MO(M = Cu、Co、Ni)复合蛋黄壳纳米球。该方法包括以适当的加热速率对Ce配位聚合物胶体球(Ce-CPCSs)进行非平衡热处理以制备CeO蛋黄壳纳米球,然后在乙醇溶液中用M(CH₃COO)₂对合成的CeO进行溶剂热处理。在溶剂热过程中,高度分散的MO物种装饰在CeO蛋黄壳纳米球的表面,形成CeO-MO复合材料。作为CO氧化催化剂,CeO-MO复合蛋黄壳纳米球由于MO和CeO之间界面处的强协同相互作用,显示出比裸CeO显著更高的催化活性。循环测试证明了这些蛋黄壳纳米球具有良好的循环稳定性。合成过程中M(CH₃COO)₂·H₂O的初始浓度对CO氧化的催化性能起着重要作用。令人印象深刻的是,在CeO-CuO₂-2样品上,在相对较低的145℃温度下实现了CO的完全转化。此外,CeO-CuO催化剂比CeO-CoO和CeO-NiO催化剂更具活性,表明催化活性与金属氧化物有关。此外,这种通用的合成方法有望创建其他具有各种结构的基于二氧化铈的复合氧化物体系,用于广泛的技术应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1f3/5704768/ce12fb147a48/Beilstein_J_Nanotechnol-08-2425-g002.jpg

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